Genetic Research Centers
Data Coordinating Center
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes.
Fine-mapping inflammatory bowel disease loci to single-variant resolution
Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.
Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Common variants at five new loci associated with early-onset inflammatory bowel disease
Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis
Common variants in the NLRP3 region contribute to Crohn's disease susceptibility
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease